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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944784Generated: October 30, 2026

Benzenepropanoyl chloride → (S)-4-BENZYL-3-(3-PHENYLPROPANOYL)OXAZOLIDIN-2-ONE

https://huagongshe.com/reaction/1944784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenepropanoyl chlorideHCID 64801—
Reactant(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(S)-4-BENZYL-3-(3-PHENYLPROPANOYL)OXAZOLIDIN-2-ONEHCID 10957844—

Reaction Steps

1.6 M of n-Butyllithium in hexanes (35 mL) was added to a solution of (S)-4-benzyloxazolidin-2-one (10 g, 56.4 mmol) in THF (150 mL) at −78° C. After 15 minutes, intermediate (7a) (9.5 g, 56.4 mmol) in THF (20 mL) was added dropwise at −78° C. After 30 minutes, the mixture was allowed to warm to room temperature and was stirred overnight. The mixture was concentrated in vacuo and the crude material was extracted with EtOAc (3×200 mL) and water (100 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated in vacuo to yield intermediate (7b), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394846B2
Source datasetuspto-grants-2013_03
ORD IDord-bd5d7d2705b74814b991a9e8aa2b21ea
Source noteuspto-grants-2013_03